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Science Immunology
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May 30, 2025
Human LY9 governs CD4<sup>+</sup> T cell IFN-γ immunity to <i>Mycobacterium tuberculosis</i>
Masato Ogishi, Julia Puchan, Rui Yang, et al.
The New England Journal of Medicine
|
June 9, 2016
Exome Sequencing and the Management of Neurometabolic Disorders
Maja Tarailo-Graovac, Casper Shyr, Colin J Ross, et al.
The Journal of Experimental Medicine
|
March 7, 2023
Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia
Ana García-García, Rebeca Pérez de Diego, Carlos Flores, et al.
Nature Genetics
|
March 30, 2024
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy
Darcy L Fehlings, Mehdi Zarrei, Worrawat Engchuan, et al.
The Journal of Experimental Medicine
|
March 8, 2023
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease
Mehul Sharma, Daniel Leung, Mana Momenilandi, et al.
Science Immunology
|
January 20, 2023
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency
, Oriol Fornes, Alicia Jia, et al.
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of 32
Search research articles
Search
Showing results (311-320 of 316) with videos related to
Sort By:
Page
of 32
You have reached the last page of results.
This site can display upto 316 results.
Science Immunology
|
May 30, 2025
Human LY9 governs CD4<sup>+</sup> T cell IFN-γ immunity to <i>Mycobacterium tuberculosis</i>
Masato Ogishi, Julia Puchan, Rui Yang, et al.
The New England Journal of Medicine
|
June 9, 2016
Exome Sequencing and the Management of Neurometabolic Disorders
Maja Tarailo-Graovac, Casper Shyr, Colin J Ross, et al.
The Journal of Experimental Medicine
|
March 7, 2023
Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia
Ana García-García, Rebeca Pérez de Diego, Carlos Flores, et al.
Nature Genetics
|
March 30, 2024
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy
Darcy L Fehlings, Mehdi Zarrei, Worrawat Engchuan, et al.
The Journal of Experimental Medicine
|
March 8, 2023
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease
Mehul Sharma, Daniel Leung, Mana Momenilandi, et al.
Science Immunology
|
January 20, 2023
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency
, Oriol Fornes, Alicia Jia, et al.
Page
of 32